ENST00000405460.9:c.12132T>G
MANE Select
|
ENSP00000384582.2:p.Asp4044Glu
|
|
ENST00000425867.3:c.1086T>G
|
ENSP00000392618.3:p.Asp362Glu
|
|
ENST00000639431.1:c.265+87107T>G
|
ENSP00000491057.1:n.265+87107T>G
|
|
ENST00000640464.1:n.2551T>G
|
|
|
ENST00000640729.1:n.709T>G
|
|
|
ENST00000405460.6:c.12132T>G
|
ENSP00000384582.2:p.Asp4044Glu
|
|
NM_032119.3:c.12132T>G
|
NP_115495.3:p.Asp4044Glu
|
|
NR_003149.1:n.12145T>G
|
|
|
XM_011543675.1:c.12129T>G
|
XP_011541977.1:p.Asp4043Glu
|
|
XM_011543676.1:c.12051T>G
|
XP_011541978.1:p.Asp4017Glu
|
|
XM_011543677.1:c.9435T>G
|
XP_011541979.1:p.Asp3145Glu
|
|
XM_011543678.1:c.12132T>G
|
XP_011541980.1:p.Asp4044Glu
|
|
NM_032119.4:c.12132T>G
MANE Select
|
NP_115495.3:p.Asp4044Glu
|
|
XM_017009963.2:c.12153T>G
|
XP_016865452.1:p.Asp4051Glu
|
|
XM_017009964.2:c.12150T>G
|
XP_016865453.1:p.Asp4050Glu
|
|
XM_017009965.1:c.12150T>G
|
XP_016865454.1:p.Asp4050Glu
|
|
XM_017009966.2:c.12072T>G
|
XP_016865455.1:p.Asp4024Glu
|
|
XM_017009967.1:c.12057T>G
|
XP_016865456.1:p.Asp4019Glu
|
|
XM_017009968.2:c.12153T>G
|
XP_016865457.1:p.Asp4051Glu
|
|
XM_017009969.2:c.12153T>G
|
XP_016865458.1:p.Asp4051Glu
|
|
XM_017009970.2:c.12153T>G
|
XP_016865459.1:p.Asp4051Glu
|
|
XM_017009971.2:c.12153T>G
|
XP_016865460.1:p.Asp4051Glu
|
|
XM_017009972.1:c.5271T>G
|
XP_016865461.1:p.Asp1757Glu
|
|
XM_017009973.1:c.5250T>G
|
XP_016865462.1:p.Asp1750Glu
|
|
NR_003149.2:n.12148T>G
|
|
|